N-substituted azetidines and other aspects of azetidine chemistry

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dc.contributor.authorLeary, G. J.en
dc.date.accessioned2014-07-20T22:10:24Z
dc.date.available2014-07-20T22:10:24Z
dc.date.issued1962en
dc.description.abstractAzetidine has been prepared and its nucleophilicity towards bromoaromatic compounds has been investigated. In this way the synthesis of a number of new N-arylazetidines has been accomplished. The infra red spectra of these azetidines, together with those of a few N-alkylazetidines, prepared from the corresponding 3-aminopropanols, have been compared. Cleavage of the 4-membered ring in N-substituted azetidines, using hydrogen bromide, has been briefly examined.en
dc.identifier.urihttp://hdl.handle.net/10092/9389
dc.identifier.urihttp://dx.doi.org/10.26021/6026
dc.language.isoen
dc.publisherUniversity of Canterbury. Chemistryen
dc.relation.isreferencedbyNZCUen
dc.rightsCopyright G. J. Learyen
dc.rights.urihttps://canterbury.libguides.com/rights/thesesen
dc.titleN-substituted azetidines and other aspects of azetidine chemistryen
dc.typeTheses / Dissertations
thesis.degree.disciplineChemistry
thesis.degree.grantorUniversity of Canterburyen
thesis.degree.levelMastersen
thesis.degree.nameMaster of Scienceen
uc.bibnumber348723
uc.collegeFaculty of Scienceen
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